REBORN ESSENCE LUMBAR FIXATION SYSTEM - CANNULATED POLY AXIAL SCREW - FDA Registration MDR-08072E

Access comprehensive regulatory information for REBORN ESSENCE LUMBAR FIXATION SYSTEM - CANNULATED POLY AXIAL SCREW in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number MDR-08072E and manufactured by Baui Biotech Co. Ltd. - New Taipei City, Taiwan R.O.C. in China. The device was registered on June 04, 2021.

This page provides complete registration details including manufacturer information, importer/distributor details (EG Healthcare, Inc.), and regulatory compliance data from the official Philippines FDA medical device database. Pure Global AI offers free access to Philippines' complete medical device registry, helping global MedTech companies navigate FDA regulations efficiently.